囊性纤维化患者在孕前和产前遗传咨询和检测方面考虑为人父母的观点。

IF 3 3区 医学 Q2 RESPIRATORY SYSTEM
Gopika Rajanikanth, Asher Prangley, Olivia M Stransky, Elinor Langfelder-Schwind, Jodie Vento, Elizabeth Felter, Traci M Kazmerski
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引用次数: 0

摘要

背景:囊性纤维化(pwCF)患者越来越多地考虑他们的生殖选择。目前,有许多基因检测方案可用于pwCF及其生殖伴侣。医疗保健提供者,包括遗传咨询师,可以教育pwCF关于这些选择,并在决策过程中支持他们。目的:探讨遗传学在pwCF生殖决策中的作用,以及他们在产前和孕前遗传咨询和检测方面的观点和经验。设计:我们对从CF基金会社区声音平台招募的年龄大于或等于18岁的pwCF美国全国样本进行了定性研究。方法:对参与者进行半结构化电话访谈并进行记录。我们利用Dedoose软件,运用归纳主题分析法对访谈笔录进行编码,引出主题。结果:我们采访了21名参与者(76.2%为女性,95.2%为白人,4.8%为西班牙裔,57.1%为父母,23.8%考虑为人父母)。关键主题包括:(1)pwCF似乎了解CF的遗传学,并且通常是由CF提供者,学校或其父母首先介绍CF遗传学;(2)母亲对生育患有CF的孩子有不同的看法;(3)部分被试在决定是否为亲生父母时,携带者检测是重要的考虑因素;(4)参与者理解遗传咨询师的作用并重视他们的知识,但只有一半的人之前见过遗传咨询师;(5) pwCF认为遗传信息应在儿童/青少年时期呈现,并在对计划生育感兴趣时加强。结论:pwCF在将CF传递给后代的问题上有不同的看法,尽管人们认识到遗传咨询的作用,并希望从基因检测中获得知识,但遗传因素只是决定亲子关系的一个因素。未来的工作应该发展基于患者、提供者或系统的干预措施,以最好地将高质量的遗传学和遗传咨询护理整合到CF团队中,为那些考虑生育的CF患者提供帮助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Perspectives of people with cystic fibrosis considering parenthood surrounding preconception and prenatal genetic counseling and testing.

Perspectives of people with cystic fibrosis considering parenthood surrounding preconception and prenatal genetic counseling and testing.

Perspectives of people with cystic fibrosis considering parenthood surrounding preconception and prenatal genetic counseling and testing.

Perspectives of people with cystic fibrosis considering parenthood surrounding preconception and prenatal genetic counseling and testing.

Background: People with cystic fibrosis (pwCF) are increasingly considering their reproductive options. Currently, there are many genetic testing options available for pwCF and their reproductive partners. Healthcare providers, including genetic counselors, can educate pwCF about these options and support them through the decision-making process.

Objective: This study explored the role of genetics in the reproductive decisions of pwCF and their perspectives and experiences surrounding prenatal and preconception genetic counseling and testing.

Design: We conducted a qualitative study of a national US sample of pwCF age ⩾18 years recruited from the CF Foundation Community Voice platform.

Methods: We conducted and recorded semi-structured telephone interviews with participants. We utilized Dedoose software and applied inductive thematic analysis to code the interview transcripts and elicit themes.

Results: We interviewed 21 participants (76.2% women, 95.2% White, 4.8% Hispanic, 57.1% parents, 23.8% considering parenthood). Key themes included: (1) pwCF appeared to understand the genetics of CF and were typically first introduced to CF genetics by CF providers, school, or their parents; (2) pwCF had diverse perspectives on having a child with CF; (3) carrier testing was an important consideration for some participants when making decisions about biological parenthood; (4) participants understood the role of genetic counselors and valued their knowledge, but only half previously met with a genetic counselor; (5) pwCF believed genetics information should be presented during childhood/adolescence and reinforced when interested in family planning.

Conclusion: pwCF have discrepant views on passing on CF to future offspring, and although there is recognition of the role of genetic counseling and a desire for knowledge from genetic testing, genetic considerations are but one factor involved in parenthood decisions. Future work should develop patient-, provider-, or system-based interventions to best integrate high-quality genetics and genetic counseling care into the CF team for those with CF considering parenthood.

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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
57
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Respiratory Disease delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of respiratory disease.
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